1. Academic Validation
  2. C-C bond formation at C-2 of a quinoline ring: synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors

C-C bond formation at C-2 of a quinoline ring: synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors

  • Bioorg Med Chem. 2012 Apr 1;20(7):2199-207. doi: 10.1016/j.bmc.2012.02.027.
K Shiva Kumar 1 S Kiran Kumar B Yogi Sreenivas Dhilli Rao Gorja Ravikumar Kapavarapu D Rambabu G Rama Krishna C Malla Reddy M V Basaveswara Rao Kishore V L Parsa Manojit Pal
Affiliations

Affiliation

  • 1 Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad 500 046, India.
Abstract

A number of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives were synthesized via AlCl(3)-mediated C-C bond forming reaction between 2-chloroquinoline-3-carbonitrile and various indoles. The methodology does not require any N-protection of the indoles employed and provided the corresponding products in good yields. The molecular structure of a representative compound was established unambiguously by single crystal X-ray diffraction and structural elaboration of a compound synthesized has been demonstrated. Many of these compounds synthesized showed PDE4 inhibitory properties in vitro. A brief structure-activity relationship studies within the series along with docking results of a representative compound (EC(50) ∼0.89 μM) is presented.

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